These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: ACE gene polymorphism in Egyptian children with idiopathic nephrotic syndrome.
    Author: Fahmy ME, Fattouh AM, Hegazy RA, Essawi ML.
    Journal: Bratisl Lek Listy; 2008; 109(7):298-301. PubMed ID: 18792483.
    Abstract:
    BACKGROUND: Idiopathic nephrotic syndrome is a common renal disease in children. ACE gene insertion/deletion (I/D) polymorphism has been studied as a predictor of clinical response to steroid therapy. OBJECTIVE: To investigate the distribution of angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism in children with idiopathic nephrotic syndrome (INS), as well as its relation with patient's clinical response to steroid therapy. METHODS: The studied subjects included 50 children with INS compared to 20 unrelated healthy children. Each individual genotype was determined using PCR amplification of extract genomic DNA and allele distribution based on size of the PCR fragments. RESULTS: Patients with INS had a significantly higher percentage of DD genotype (p < 0.05) than the control group. D allele frequency was significantly higher in INS patients than healthy controls. CONCLUSION: Our results showed that INS is associated with a higher incidence of DD genotype, especially in non-SS patients. This data suggested that DD genotype may play a role in the clinical response to steroid. Angiotensin II may be involved in part in the response to steroid treatment in children with INS (Tab. 4, Fig. 1, Ref. 20).
    [Abstract] [Full Text] [Related] [New Search]